| Literature DB >> 18971529 |
Tong Yin1, Keiko Maekawa, Kei Kamide, Yoshiro Saito, Hironori Hanada, Kotaro Miyashita, Yoshihiro Kokubo, Yasuhisa Akaiwa, Ryoichi Otsubo, Kazuyuki Nagatsuka, Toshiho Otsuki, Takeshi Horio, Shin Takiuchi, Yuhei Kawano, Kazuo Minematsu, Hiroaki Naritomi, Hitonobu Tomoike, Jun-ichi Sawada, Toshiyuki Miyata.
Abstract
CYP2C9, a drug-metabolizing enzyme, converts the angiotensin II receptor blocker losartan to its active form, which is responsible for its antihypertensive effect. We resequenced CYP2C9 in 724 Japanese individuals, including 39 hypertensive patients under treatment with losartan. Of two novel missense mutations identified, the Arg132Gln variant showed a fivefold lower intrinsic clearance toward diclofenac when expressed in a baculovirus-insect cell system, while the Arg335Gln variant had no substantial effect. Several known missense variations were also found, and approximately 7% of the Japanese individuals (53 out of 724) carried one of the deleterious alleles (CYP2C9*3, *13, *14, *30, and Arg132Gln) as heterozygotes. After 3 months of losartan treatment, systolic blood pressure was not lowered in two patients with CYP2C9* 1/*30, suggesting that they exhibited impaired in vivo CYP2C9 activity. CYP2C9*30 might be associated with a diminished response to the antihypertensive effects of losartan.Entities:
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Year: 2008 PMID: 18971529 DOI: 10.1291/hypres.31.1549
Source DB: PubMed Journal: Hypertens Res ISSN: 0916-9636 Impact factor: 3.872